Disease #06096 (NOCGUS (Neurooculocardiogenitourinary syndrome), OMIM:618652)

Official abbreviation NOCGUS
Name Neurooculocardiogenitourinary syndrome
OMIM ID 618652
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene WDR37
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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